Brain monitor may predict easier breathing tube placement in ER

NCT ID NCT07690254

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First seen Jul 08, 2026 · Last updated Jul 09, 2026 · Updated 1 time

Summary

This study observes whether the depth of anesthesia, measured by a brain activity monitor (BIS), affects how easily a breathing tube can be placed on the first try in emergency room patients. Adults undergoing rapid sequence intubation will wear a forehead sensor, but doctors will not see the readings. The goal is to see if patients who need multiple attempts have different anesthetic depth than those who succeed on the first try.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If a link is found, it could help doctors optimize sedation for safer intubation in emergencies.
What could go wrong
This is an observational study, so it cannot prove cause and effect. Results may not change practice directly.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 150 people

The number the study aims to enrol. It can still change while the study runs.

Started

May 2026

Expected to finish

May 2028

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Adult patients ındergoing RSı in the ED

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Adults aged 18 years or older * Patients undergoing rapid sequence intubation (RSI) in the emergency department * No traumatic injury to the frontal region that would interfere with placement of the Bispectral Index (BIS) sensor Exclusion Criteria: * Age younger than 18 years * Pregnant patients * Patients with cardiac arrest or hemodynamic instability at the time of enrollment * Patients intubated without the rapid sequence intubation (RSI) protocol * Refusal to participate in the study (by the patient or, where applicable, a legally authorized representative)

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As listed by the trial registrant

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How to take part

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  2. The official record

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Contacts and locations

Locations

  • Akdeniz University Hospital

    RECRUITING

    Antalya, 07059, Turkey (Türkiye)

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